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  • 1985-1989  (2)
  • Polymer and Materials Science  (2)
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  • 1985-1989  (2)
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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 27 (1989), S. 2357-2366 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: p-Divinylbenzene (DVB) 13C-labeled at the methine carbon of the vinyl group was copolymerized in suspension with styrene at 70, 70-95, and 135-155°C using 2,2′-azobisisobutyronitrile (AIBN) as the initiator. The number of unreacted vinyl groups in each copolymer was determined by 13C CP-MAS NMR analysis of solid samples, direct polarization 13C-NMR analysis of CDCl3-swollen gels, and bromination. Results from the three methods agree methods agree qualitatively. Even the 1% DVB-crosslinked networks contained 40% unreacted DVB-vinyl groups when prepared by high conversion polymerization at 70°C and 16% unreacted DVB-vinyl groups when polymerization was finished at 95°C. The analyses were also applied to some commercial crosslinked polystyrenes. Every sample examined contained pendent vinyl groups
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 27 (1989), S. 2345-2355 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Cross-polarization magic-angle-spinning 13C-NMR spectra of polystyrenes crosslinked with 1-20% of methine vinyl carbon 13C-labeled p-divinylbenzene and of Friedel-Crafts crosslinked poly(chloromethylstyrene)s have been obtained with both glossy solid and CDCl3-swollen gel samples. The spectra of natural abundance, uncrosslinked, glassy polystyrene, and the spectra of the solid labeled networks give aliphatic and aromatic peak areas only 0.7 times as large per 13C atom as that of poly(oxymethylene). Similarly the crosslinked poly(chloromethylstyrene) gave peak areas about 0.6 times that of internal poly(oxymethylene). The labeled gels give peak areas 0.2-0.6 times as large per 13C atom as glassy polystyrene, and the peak areas in spectra of gels increase with the divinylbenzene content
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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